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Ready to make a real impact on quality, compliance and patient care? Here at Curaleaf Laboratories, we’re looking for an experienced Senior Quality Assurance Officer to join our Quality team and play a key role in maintaining and continuously improving our Quality Management System (QMS). As a leading UK manufacturer and distributor of EU-GMP medical cannabis, quality is at the heart of everything we do. You’ll have the opportunity to apply your QA expertise within a growing and evolving industry, helping ensure that pharmaceutical‑grade medical cannabis products meet the highest standards of quality, safety and compliance. This is an excellent opportunity for an experienced QA professional looking to take on greater responsibility, provide leadership within the QA function and make a real impact on quality and compliance across the business. This role is on‑site in Sunderland, England. About us: Curaleaf International is shaping the future of cannabis through its commitment to research and product excellence. Powered by a strong presence at all stages of the supply chain, its unique distribution network throughout Europe, Canada and Australasia brings together pioneering research with cutting‑edge cultivation, extraction, and production. Amidst a rapid growth trajectory, the emphasis on quality and expertise aims to ensure the delivery of safe and legal cannabis. Curaleaf International’s network includes a clinic, pharmacy, and laboratory in the UK; cultivation and EU‑GMP processing facilities in Portugal; an EU‑GMP processing, quality assurance and research site in Spain; Four 20 Pharma wholesaler and distributor in Germany; a Polish wholesaler and clinic; and the EU‑GMP producer Northern Green Canada. Curaleaf International is part of Curaleaf Holdings, Inc., a leading international producer and distributor of consumer cannabis products. As Senior Quality Assurance Officer, you will provide management and support across quality activities relating to GMP and GDP, helping to ensure the business maintains high standards of regulatory compliance across manufacturing and distribution operations. You will work closely with Quality, Production, Warehouse and other teams, providing guidance and support while helping to develop a strong culture of continuous quality improvement. As a senior member of the QA team, you will mentor and support colleagues and deputise for the QA Manager when required. About Us Curaleaf International is shaping the future of cannabis through its commitment to research and product excellence. Powered by a strong presence at all stages of the supply chain, its unique distribution network throughout Europe, Canada and Australasia brings together pioneering research with cutting‑edge cultivation, extraction, and production. Amidst a rapid growth trajectory, the emphasis on quality and expertise aims to ensure the delivery of safe and legal cannabis. Curaleaf International’s network includes a clinic, pharmacy, and laboratory in the UK; cultivation and EU‑GMP processing facilities in Portugal; an EU‑GMP processing, quality assurance and research site in Spain; Four 20 Pharma wholesaler and distributor in Germany; a Polish wholesaler and clinic; and the EU‑GMP producer Northern Green Canada. Curaleaf International is part of Curaleaf Holdings, Inc., a leading international producer and distributor of consumer cannabis products. • Manage and support the Quality Management System (QMS), including deviations, CAPAs, change controls, recalls, complaints and audits., • Lead root cause analysis (RCA) for quality events, OOS results and customer complaints, ensuring effective CAPAs are implemented., • Monitor quality KPIs, identify trends and provide clear quality reports to management., • Support and participate in customer and regulatory audits, including responding to audit findings., • Ensure GMP and GDP requirements are maintained across manufacturing and distribution activities., • Promote and enforce SOPs, policies, procedures and controlled documentation., • Mentor and support QA team members and contribute to a strong culture of continuous quality improvement., • Support quality training across Quality, Production and Warehouse teams., • Work collaboratively with cross‑functional teams to identify risks and improve quality processes., • Deputise for the QA Manager when required. We are looking for an experienced QA professional with: • 5+ years' experience in Quality Assurance or a similar role., • Experience leading, managing or mentoring a team, or providing support in a senior/lead capacity., • A degree in Science or a related discipline., • Strong experience with RCA, CAPAs, deviations, audits and quality metrics., • Experience working within a regulated GMP/GDP environment., • Demonstrable experience managing quality risks and supporting continuous improvement., • Experience dealing with customer and/or regulatory audits and challenging audit findings., • Strong communication, presentation and reporting skills., • The confidence to influence and collaborate with cross‑functional teams and senior management., • A calm, practical and organised approach, with strong decision‑making and prioritisation skills. You’ll be someone who takes ownership, works confidently and can build strong relationships while maintaining a clear focus on quality, compliance and continuous improvement. You’ll be joining a growing Quality function at an important stage in its development, with the opportunity to influence quality standards, support new projects and validations, and help shape continuous improvement across the business. This is a great opportunity for someone looking to develop their career within a senior QA position, with the opportunity to provide leadership, mentor colleagues and contribute to the ongoing development of Curaleaf's quality culture. #J-18808-Ljbffr

Occupational Health Physician - Chief Medical Officer Occupational Health Houghton Le Spring Permanent Nov 5, 2026 Remote Role | 1 Day Per Month On-Site | Competitive Day Rate Are you an experienced Occupational Health Physician looking for a strategic leadership opportunity with flexibility, influence, and the ability to shape clinical excellence? We are seeking a highly credible and experienced Chief Medical Officer (CMO) to provide clinical leadership across a well-established Occupational Health service. This is a predominantly remote position, requiring attendance in Houghton-le-Spring once per month, offering an excellent opportunity to make a significant impact while maintaining flexibility. As Chief Medical Officer, you will play a pivotal role in providing clinical direction, governance, and expert guidance across our Occupational Health operations. Working closely with the Head of Occupational Health Operations, you will ensure services are delivered to the highest clinical standards and in line with industry best practice. This is an influential appointment for a senior Occupational Health professional who enjoys supporting clinicians, driving quality, and contributing to service development. • Provide expert clinical leadership and advice across the Occupational Health function., • Undertake clinical work to the highest professional standards when required., • Support quality assurance through clinical audits, peer reviews, and report assessments., • Provide guidance on clinical queries, complaints, and complex case management., • Contribute clinical expertise during tender processes and service design discussions., • Support and actively participate in clinical governance activities., • Review clinical trends and audit findings to improve service quality and consistency., • Help develop policies, procedures, and best-practice frameworks., • Provide education, mentoring, and professional support to Occupational Health colleagues., • Remain up to date with legislative, regulatory, and professional changes affecting Occupational Health practice. To be successful in this role, you will possess: • Full GMC registration., • MFOM, AFOM, or equivalent Occupational Health qualification., • Strong understanding of clinical governance and quality assurance frameworks., • Sound knowledge of GDPR, Data Protection, and Information Governance requirements., • Significant experience across a broad range of Occupational Health settings., • Strong report-writing and clinical assessment skills., • Experience conducting clinical audits and quality reviews., • Excellent knowledge of Occupational Health legislation, HSE guidance, and associated regulations., • Experience providing senior clinical advice and guidance to multidisciplinary teams., • A credible and respected clinical leader with natural gravitas., • Strong communicator with exceptional written and verbal skills., • Confident in managing differing professional opinions and reaching balanced outcomes., • Passionate about quality improvement, education, and clinical excellence., • Organised, pragmatic, and solutions-focused., • Committed to supporting and developing colleagues., • Highly competitive day rate, • Predominantly remote working, • Just one on-site visit per month in Houghton-le-Spring, • Opportunity to influence and shape Occupational Health strategy and governance, • Work alongside an experienced and collaborative leadership team If you are an accomplished Occupational Health Physician looking for a flexible senior leadership opportunity where your expertise will directly influence clinical excellence and service delivery, we would be delighted to hear from you. #J-18808-Ljbffr

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